The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score
Author:
Publisher
Wiley
Subject
Hematology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1600-0609.2011.01705.x/fullpdf
Reference21 articles.
1. Predicting clinical severity in sickle cell anaemia;Steinberg;Br J Haematol,2005
2. Development and validation of a pediatric severity index for sickle cell patients;van den Tweel;Am J Hematol,2010
3. Development and evaluation of a sickle cell assessment instrument;Day;Pediatr Nurs,2004
4. Rapid and reliable beta-globin gene cluster haplotyping of sickle cell disease patients by FRET Light Cycler and HRM assays;Joly;Clin Chim Acta,2011
5. Single-tube multiplex-PCR screen for common deletional determinants of alpha-thalassemia;Chong;Blood,2000
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1. Genetic Variation and Sickle Cell Disease Severity;JAMA Network Open;2023-10-18
2. Genetic Modifiers of Sickle Cell Disease;Hematology/Oncology Clinics of North America;2022-12
3. The pleiotropic effects of α‐thalassemia on HbSS and HbSC sickle cell disease: Reduced erythrocyte cation co‐transport activity, serum erythropoietin, and transfusion burden, do not translate into increased survival;American Journal of Hematology;2022-07-18
4. Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort;Annals of Hematology;2021-02-13
5. Influence of beta-cluster haplotypes, alpha-gene status and UGTA1 polymorphism on clinical and hematological data in sickle-cell disease children from French Guiana;PLOS ONE;2020-09-03
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